Variant report

Variant	nsv948436
Chromosome Location	chr8:51115028-51917504
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1616)
CpG islands
(count:673)
Chromatin interactive
region (count:33)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1616 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:51351100-51351279	HepG2	liver:	n/a	n/a
2	ATF1	chr8:51210088-51210191	K562	blood:	n/a	n/a
3	ATF3	chr8:51310791-51311060	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF3	chr8:51310742-51311085	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF3	chr8:51310845-51311121	K562	blood:	n/a	n/a
6	BACH1	chr8:51322783-51322854	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr8:51380375-51380444	K562	blood:	n/a	n/a
8	BACH1	chr8:51360829-51360868	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr8:51204453-51204562	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr8:51760453-51760811	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr8:51760452-51760813	K562	blood:	n/a	n/a
12	BACH1	chr8:51549746-51549863	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr8:51448363-51448441	K562	blood:	n/a	n/a
14	BACH1	chr8:51622516-51622751	H1-hESC	embryonic stem cell:	n/a	chr8:51622657-51622671
15	BACH1	chr8:51551406-51551486	H1-hESC	embryonic stem cell:	n/a	n/a
16	BHLHE40	chr8:51310826-51311066	K562	blood:	n/a	n/a
17	BHLHE40	chr8:51553900-51554065	GM12878	blood:	n/a	n/a
18	BHLHE40	chr8:51310789-51311051	HepG2	liver:	n/a	n/a
19	BRCA1	chr8:51771806-51771914	Hela-S3	cervix:	n/a	n/a
20	BRCA1	chr8:51310893-51310975	H1-hESC	embryonic stem cell:	n/a	n/a
21	CEBPB	chr8:51167269-51167657	Hela-S3	cervix:	n/a	chr8:51167453-51167470
22	CEBPB	chr8:51199867-51200122	H1-hESC	embryonic stem cell:	n/a	chr8:51199988-51199999
23	CEBPB	chr8:51284262-51284449	A549	lung:	n/a	n/a
24	CEBPB	chr8:51417321-51417664	Hela-S3	cervix:	n/a	chr8:51417510-51417521 chr8:51417479-51417490
25	CEBPB	chr8:51576308-51576662	IMR90	lung:	n/a	n/a
26	CEBPB	chr8:51384894-51385137	IMR90	lung:	n/a	n/a
27	CEBPB	chr8:51301753-51301900	K562	blood:	n/a	chr8:51301857-51301868
28	CEBPB	chr8:51774506-51774533	H1-hESC	embryonic stem cell:	n/a	n/a
29	CEBPB	chr8:51137953-51138297	IMR90	lung:	n/a	chr8:51138124-51138135
30	CEBPB	chr8:51755011-51755229	H1-hESC	embryonic stem cell:	n/a	n/a
31	CEBPB	chr8:51755059-51755254	HepG2	liver:	n/a	n/a
32	CEBPB	chr8:51306294-51306472	A549	lung:	n/a	chr8:51306433-51306444
33	CEBPB	chr8:51310815-51311070	A549	lung:	n/a	chr8:51310953-51310964
34	CEBPB	chr8:51167319-51167607	MCF-7	breast:	n/a	chr8:51167453-51167470
35	CEBPB	chr8:51340892-51341151	H1-hESC	embryonic stem cell:	n/a	chr8:51341047-51341056 chr8:51341045-51341058 chr8:51341047-51341056 chr8:51341045-51341056 chr8:51341045-51341058 chr8:51341047-51341056 chr8:51341045-51341058 chr8:51341046-51341057 chr8:51341047-51341056 chr8:51341045-51341056
36	CEBPB	chr8:51217230-51217472	H1-hESC	embryonic stem cell:	n/a	chr8:51217369-51217380
37	CEBPB	chr8:51306357-51306493	HepG2	liver:	n/a	chr8:51306433-51306444
38	CEBPB	chr8:51417303-51417661	K562	blood:	n/a	chr8:51417510-51417521 chr8:51417479-51417490
39	CEBPB	chr8:51176238-51176491	A549	lung:	n/a	chr8:51176300-51176311
40	CEBPB	chr8:51853747-51854039	IMR90	lung:	n/a	n/a
41	CEBPB	chr8:51320425-51320659	HepG2	liver:	n/a	chr8:51320549-51320560
42	CEBPB	chr8:51153154-51153293	H1-hESC	embryonic stem cell:	n/a	chr8:51153238-51153251
43	CEBPB	chr8:51293479-51293710	HepG2	liver:	n/a	n/a
44	CEBPB	chr8:51176175-51176483	IMR90	lung:	n/a	chr8:51176300-51176311
45	CEBPB	chr8:51463151-51463193	HepG2	liver:	n/a	n/a
46	CEBPB	chr8:51310785-51311240	MCF-7	breast:	n/a	chr8:51310953-51310964
47	CEBPB	chr8:51741406-51741719	A549	lung:	n/a	chr8:51741562-51741573 chr8:51741528-51741539
48	CEBPB	chr8:51293521-51293731	A549	lung:	n/a	n/a
49	CEBPB	chr8:51212701-51212837	H1-hESC	embryonic stem cell:	n/a	n/a
50	CEBPB	chr8:51217189-51217557	IMR90	lung:	n/a	chr8:51217369-51217380

(count:673 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:51555740-51555790	IMR90	lung:	fetal
2	chr8:51555740-51555790	HMEC	breast:	n/a
3	chr8:51555740-51555790	IMR90	lung:	fetal
4	chr8:51555740-51555790	HMEC	breast:	n/a
5	chr8:51364244-51364294	BE2_C	brain:	n/a
6	chr8:51576109-51576159	T-47D	breast:	n/a
7	chr8:51404106-51404156	T-47D	breast:	n/a
8	chr8:51199947-51199997	SK-N-SH_RA	brain:	n/a
9	chr8:51555740-51555790	HL-60	blood:	n/a
10	chr8:51555740-51555790	NH-A	brain:	n/a
11	chr8:51404179-51404229	AG09309	skin:	n/a
12	chr8:51449266-51449316	HL-60	blood:	n/a
13	chr8:51404106-51404156	IMR90	lung:	fetal
14	chr8:51404066-51404116	AoSMC	blood vessel:	n/a
15	chr8:51555740-51555790	HPAEpiC	pulmonary alveolar:	n/a
16	chr8:51449266-51449316	AG04450	lung:	fetal
17	chr8:51404106-51404156	ECC-1	luminal epithelium:	n/a
18	chr8:51553739-51553789	AG04450	lung:	fetal
19	chr8:51576109-51576159	HNPCEpiC	eye:	n/a
20	chr8:51553739-51553789	HCT-116	colon:	n/a
21	chr8:51364244-51364294	AG04450	lung:	fetal
22	chr8:51555740-51555790	H1-hESC	embryonic stem cell:	embryo
23	chr8:51528401-51528451	PrEC	prostate:	n/a
24	chr8:51404066-51404116	U87	brain:	n/a
25	chr8:51404179-51404229	MCF10A-Er-Src	breast:	n/a
26	chr8:51553739-51553789	H1-hESC	embryonic stem cell:	embryo
27	chr8:51364244-51364294	U87	brain:	n/a
28	chr8:51404179-51404229	LNCaP	prostate:	n/a
29	chr8:51288552-51288602	SAEC	small airway:	n/a
30	chr8:51288552-51288602	HCT-116	colon:	n/a
31	chr8:51288552-51288602	CMK	blood:	n/a
32	chr8:51576109-51576159	ovcar-3	ovarian:	n/a
33	chr8:51528401-51528451	NB4	blood:	n/a
34	chr8:51404179-51404229	GM06990	blood:	n/a
35	chr8:51288552-51288602	A549	lung:	n/a
36	chr8:51555740-51555790	HCM	heart:	n/a
37	chr8:51404106-51404156	HRE	kidney:	n/a
38	chr8:51404066-51404116	GM06990	blood:	n/a
39	chr8:51288552-51288602	GM06990	blood:	n/a
40	chr8:51404066-51404116	PANC-1	pancreas:	n/a
41	chr8:51553739-51553789	NH-A	brain:	n/a
42	chr8:51199947-51199997	Hepatocyte	liver:	n/a
43	chr8:51364244-51364294	HUVEC	blood vessel:	n/a
44	chr8:51528401-51528451	SK-N-MC	brain:	n/a
45	chr8:51404066-51404116	CMK	blood:	n/a
46	chr8:51576109-51576159	AG09319	gingival:	n/a
47	chr8:51199947-51199997	AG04450	lung:	fetal
48	chr8:51576109-51576159	NB4	blood:	n/a
49	chr8:51528401-51528451	HepG2	liver:	n/a
50	chr8:51364244-51364294	Hepatocyte	liver:	n/a

(count:33 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:135846774..135848617-chr8:51481190..51483855,2	MCF-7	breast:
2	chr8:51677159..51678716-chr8:51680516..51682123,2	K562	blood:
3	chr1:116959143..116962126-chr8:51573809..51576471,2	MCF-7	breast:
4	chr8:51219065..51222213-chr8:51225649..51228332,3	K562	blood:
5	chr8:51711545..51713227-chr8:51715658..51718026,2	K562	blood:
6	chr1:144893909..144894771-chr8:51229590..51230343,2	MCF-7	breast:
7	chr8:51700925..51703034-chr8:51706252..51708028,2	K562	blood:
8	chr8:51187159..51189399-chr8:51189828..51191872,2	MCF-7	breast:
9	chr8:51854395..51855974-chr8:51858657..51860193,2	K562	blood:
10	chr8:51194558..51197541-chr8:51202196..51204695,2	MCF-7	breast:
11	chr8:51219065..51222213-chr8:51225649..51228332,3	K562	blood:
12	chr8:50826287..50827033-chr8:51310198..51311230,3	MCF-7	breast:
13	chr8:51590048..51591794-chr8:51592149..51596284,3	K562	blood:
14	chr8:51590048..51591794-chr8:51592149..51596284,3	K562	blood:
15	chr8:51464363..51466671-chr8:51475999..51477985,2	K562	blood:
16	chr8:51372315..51374214-chr8:51375832..51377998,2	K562	blood:
17	chr8:51194558..51197541-chr8:51202196..51204695,2	MCF-7	breast:
18	chr8:51715941..51718504-chr8:51718568..51721133,2	K562	blood:
19	chr8:51372315..51374214-chr8:51375832..51377998,2	K562	blood:
20	chr8:51187159..51189399-chr8:51189828..51191872,2	MCF-7	breast:
21	chr8:51715941..51718504-chr8:51718568..51721133,2	K562	blood:
22	chr8:51767065..51768781-chr8:51770684..51773527,2	MCF-7	breast:
23	chr8:49891255..49891972-chr8:51310445..51311051,2	MCF-7	breast:
24	chr8:51252100..51253925-chr8:51256216..51258662,2	MCF-7	breast:
25	chr8:51252100..51253925-chr8:51256216..51258662,2	MCF-7	breast:
26	chr8:50947214..50948091-chr8:51310516..51311364,3	MCF-7	breast:
27	chr8:51677159..51678716-chr8:51680516..51682123,2	K562	blood:
28	chr13:32746778..32747333-chr8:51314361..51315226,2	MCF-7	breast:
29	chr8:50947077..50947745-chr8:51310573..51311162,2	MCF-7	breast:
30	chr8:51711545..51713227-chr8:51715658..51718026,2	K562	blood:
31	chr8:51700925..51703034-chr8:51706252..51708028,2	K562	blood:
32	chr8:51854395..51855974-chr8:51858657..51860193,2	K562	blood:
33	chr8:50753724..50754320-chr8:51310816..51311345,2	MCF-7	breast:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C8orf22-6	chr8:51293575-51293638	ENSG00000253849.1
2	lnc-SNTG1-2	chr8:51772090-51772622	NONHSAT126530
3	lnc-C8orf22-6	chr8:51294466-51294835	ENSG00000253849.1
4	lnc-C8orf22-15	chr8:51199098-51199413	NONHSAT126524
5	lnc-PXDNL-4	chr8:51675020-51675358	NONHSAT126529

No data

Variant related genes	Relation type
ENSG00000254392	TF binding region
ENSG00000253340	TF binding region
ENSG00000253849	TF binding region
CYCSP22	TF binding region
SNTG1	TF binding region
ENSG00000254392	CpG island
ENSG00000253340	CpG island
ENSG00000253849	CpG island
CYCSP22	CpG island
SNTG1	CpG island
ENSG00000203865	chromatin interactions
ENSG00000253340	chromatin interactions
ENSG00000147481	chromatin interactions

Extended variants
information (count: 19353 )
Associated
traits (count: 98 )

Variant overlapped rSNPs/rCNVs (count:19353 , 50 per page) page: 1 2 3 4 5 6 7 ... 388

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7016161	chr8:51115028-51115029	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs7001922	chr8:51115049-51115050	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs573869740	chr8:51115076-51115077	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs188448999	chr8:51115162-51115163	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs143645767	chr8:51115223-51115224	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs543341795	chr8:51115243-51115244	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs559922270	chr8:51115260-51115261	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs193228353	chr8:51115268-51115269	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs577831677	chr8:51115269-51115270	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs528565369	chr8:51115295-51115296	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs60509732	chr8:51115356-51115357	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs538992734	chr8:51118023-51118024	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs557394206	chr8:51118025-51118026	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs78997621	chr8:51118033-51118034	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs536757073	chr8:51118034-51118035	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs146827760	chr8:51118046-51118047	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs139599414	chr8:51118052-51118053	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs183816416	chr8:51118055-51118056	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs559030689	chr8:51118068-51118069	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs188753496	chr8:51118076-51118077	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs543761082	chr8:51118087-51118088	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs192493557	chr8:51118098-51118099	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs565290460	chr8:51118107-51118108	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs142943353	chr8:51118164-51118165	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs541560175	chr8:51118185-51118186	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs4873426	chr8:51121611-51121612	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs562343116	chr8:51121618-51121619	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs4873131	chr8:51121619-51121620	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs548375407	chr8:51121624-51121625	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs192613864	chr8:51121633-51121634	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs7835849	chr8:51121643-51121644	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs182603696	chr8:51121649-51121650	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs571694717	chr8:51121662-51121663	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs575701046	chr8:51121667-51121668	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs7817040	chr8:51121692-51121693	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs71511987	chr8:51121718-51121719	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs551135787	chr8:51121727-51121728	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs187311153	chr8:51121743-51121744	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs373291238	chr8:51121744-51121745	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs569189834	chr8:51121762-51121763	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs536397455	chr8:51121775-51121776	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs10105597	chr8:51121786-51121787	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs192126964	chr8:51121790-51121791	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs534252673	chr8:51121824-51121825	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs574926442	chr8:51121848-51121849	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs558111378	chr8:51121860-51121861	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs576479342	chr8:51121863-51121864	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs543897967	chr8:51121880-51121881	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs562207040	chr8:51121902-51121903	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs370296652	chr8:51121903-51121904	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:98)

Disease	PMID	Source
Cancer	16751803	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Ewing''s sarcoma	21437220	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Seminomas	18059402	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pancreatic cancer	21811587	CNVD
Multiple myeloma	16461302	CNVD
Developmental delay	21373258	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Disorders of sex development	21048976	CNVD
Testicular cancer	18059402	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Cancer	20164919	CNVD
primary effusion lymphomas	17116491	CNVD
Esophageal cancer	20955586	CNVD
abnormal development	18461090	CNVD
Cancer	20164920	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Oral cancer	21386901	CNVD
Uveal melanoma	21693616	CNVD
Langer-Giedion syndrome	22283845	CNVD
Cancer	21637783	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	20632083	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	19627613	CNVD
Prostate cancer	21088497	CNVD
colon cancer	17210682	CNVD
Breast cancer	21264507	CNVD
Breast cancer	22028636	CNVD
Acute myeloid leukemia	16864856	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Gastric cancer	17167181	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	16461572	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
head and neck squamous cell carcinoma	18028549	CNVD
Breast cancer	17001317	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Acute myeloid leukemia	21251322	CNVD
Glioblastoma multiforme	22286061	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Melanoma	17363583	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	18628472	CNVD
Sezary syndrome	18413736	CNVD
Ovarian cancer	22174824	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
early-passage human iPS cells	21368824	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Type 1 diabetes	21085585	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
22q11 deletion syndrome	20357662	CNVD
Medulloblastoma	21163964	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:677 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:51114800-51115400	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr8:51118000-51118200	Enhancers	Pancreatic Islets	Pancreatic Islet
3	chr8:51121600-51122200	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
4	chr8:51122200-51124800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
5	chr8:51124000-51125800	Enhancers	Cortex derived primary cultured neurospheres	brain
6	chr8:51124800-51125800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
7	chr8:51124800-51126000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr8:51125000-51125400	Enhancers	Fetal Brain Female	brain
9	chr8:51125000-51125600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chr8:51125000-51125600	Enhancers	Brain Anterior Caudate	brain
11	chr8:51125000-51125800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr8:51125000-51125800	Enhancers	Brain Germinal Matrix	brain
13	chr8:51125000-51126000	Enhancers	Osteobl	bone
14	chr8:51125400-51125800	Enhancers	Fetal Lung	lung
15	chr8:51125800-51127200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
16	chr8:51127200-51127400	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
17	chr8:51127400-51127600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
18	chr8:51134400-51135200	ZNF genes & repeats	Liver	Liver
19	chr8:51142000-51143200	Enhancers	Liver	Liver
20	chr8:51153200-51153800	Active TSS	Liver	Liver
21	chr8:51153800-51154600	Flanking Active TSS	Liver	Liver
22	chr8:51154600-51155000	Enhancers	Liver	Liver
23	chr8:51156600-51156800	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
24	chr8:51156800-51161400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
25	chr8:51160200-51167200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr8:51161400-51162400	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
27	chr8:51161600-51162000	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr8:51161800-51162200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
29	chr8:51161800-51162200	ZNF genes & repeats	Cortex derived primary cultured neurospheres	brain
30	chr8:51170000-51170800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
31	chr8:51172400-51173200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr8:51172800-51173200	Active TSS	Fetal Heart	heart
33	chr8:51192200-51192800	Enhancers	Liver	Liver
34	chr8:51192200-51194200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
35	chr8:51193600-51195000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr8:51194200-51194400	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
37	chr8:51198600-51200600	Enhancers	HUES48 Cell Line	embryonic stem cell
38	chr8:51198800-51199200	Enhancers	H9 Cell Line	embryonic stem cell
39	chr8:51198800-51199400	Enhancers	iPS-18 Cell Line	embryonic stem cell
40	chr8:51198800-51200000	Enhancers	ES-I3 Cell Line	embryonic stem cell
41	chr8:51198800-51200200	Enhancers	HUES6 Cell Line	embryonic stem cell
42	chr8:51198800-51200400	Enhancers	iPS-20b Cell Line	embryonic stem cell
43	chr8:51199000-51199200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
44	chr8:51199200-51200000	Weak transcription	H9 Cell Line	embryonic stem cell
45	chr8:51199200-51200800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
46	chr8:51199400-51199800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
47	chr8:51199400-51200400	Enhancers	HUES64 Cell Line	embryonic stem cell
48	chr8:51199600-51200400	Enhancers	iPS-15b Cell Line	embryonic stem cell
49	chr8:51199800-51200200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr8:51199800-51200200	Enhancers	iPS-18 Cell Line	embryonic stem cell

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